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The April 2016 JEADV issue covered various dermatology topics, including psoriasis, psoriatic arthritis, mTOR inhibitors, autoimmune diseases, photodynamic therapy, viral DNA in skin diseases, chronic hand eczema, and female hair loss.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Soft-tissue calcification is rare in systemic lupus erythematosus.

Finasteride effectively treated hidradenitis suppurativa.

Post-Exposure Syndromes are persistent conditions caused by past exposures, needing unique interventions.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Psychodermatosis is reclassified based on brain-skin interaction, dividing conditions into psychogenic and psychosomatic categories.

A rare neck cyst in a 47-year-old man showed diverse skin cell types and was not linked to HPV.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Fine wool sheep have more genes for wool quality, while coarse wool sheep have more for skin and muscle traits.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Breast cancer alters specific molecular structures in hair, which revert after cancer removal.

New compounds may help treat prostate cancer by reducing cell growth.

MRI helps distinguish between pituitary adenomas and craniopharyngiomas, guides treatment for pediatric CNS tumors, and assesses rhinocerebral mucormycosis with a high mortality rate in transplanted patients.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Multiple trichofolliculomas can look like multiple trichoepitheliomas on the face.

Post-exposure syndromes are persistent conditions caused by past exposures, needing unique interventions.

The conclusion is that self-concept, shame, and emotion regulation are key factors in hoarding disorder, body dysmorphic disorder, and trichotillomania, and should be targeted in treatment and research.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Two new gene mutations cause a rare hair disorder.